The JI PBL Intereron Source
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Go, C.
Right arrow Articles by Miller, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Go, C.
Right arrow Articles by Miller, J.

The Journal of Immunology, Vol 150, Issue 2 367-376, Copyright © 1993 by American Association of Immunologists


ARTICLES

Anergized T cell clones retain their cytolytic ability

C Go, DW Lancki, FW Fitch and J Miller
Department of Pathology, University of Chicago, IL 60637.

CD4+ T cells have been described to have both helper and lytic function. The helper function of Th1 cells in particular can be inactivated by inducing the T cell into a state of nonresponsiveness in which the T cell is no longer capable of producing IL-2 or proliferating in an autocrine way to a conventional antigenic stimulus. To determine whether the lytic ability of Th1 cells can also be rendered nonfunctional upon anergy induction, we induced Th1 clones into a nonresponsive state and tested their ability to lyse target cells in an Ag-specific and MHC class II-restricted manner. We show that cells newly induced into an anergic state were able to lyse target cells nonspecifically. This effect was short-lived and after resting in culture media, the cells regained their ability to lyse target cells in an Ag/MHC-specific manner, and this ability was comparable to normal resting T cells. In contrast, the helper function of these cells remained nonresponsive, and the cells were unable to proliferate or to secrete IL-2 in response to the same antigenic stimulus used for lysis. Therefore, the lytic pathway appears to be regulated separately from the proliferative/lymphokine pathway(s) and is not affected long-term by an anergic stimulus.


This article has been cited by other articles:


Home page
J. Immunol.Home page
P. A. Taylor, A. Panoskaltsis-Mortari, R. J. Noelle, and B. R. Blazar
Analysis of the Requirements for the Induction of CD4+ T Cell Alloantigen Hyporesponsiveness by Ex Vivo Anti-CD40 Ligand Antibody
J. Immunol., January 15, 2000; 164(2): 612 - 622.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
S. Sad and L. Krishnan
Cytokine Deprivation of Naive CD8+ T Cells Promotes Minimal Cell Cycling but Maximal Cytokine Synthesis and Autonomous Proliferation Subsequently: A Mechanism of Self-Regulation
J. Immunol., September 1, 1999; 163(5): 2443 - 2451.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
L. A. Zuckerman, L. Pullen, and J. Miller
Functional Consequences of Costimulation by ICAM-1 on IL-2 Gene Expression and T Cell Activation
J. Immunol., April 1, 1998; 160(7): 3259 - 3268.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
G Lombardi, S Sidhu, R Batchelor, and R Lechler
Anergic T cells as suppressor cells in vitro
Science, June 10, 1994; 264(5165): 1587 - 1589.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1993 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1993 by The American Association of Immunologists, Inc. All rights reserved.